Assistant Clinical Research Coordinator
The Department of Radiation Oncology is hiring an Assistant Clinical Research Coordinator to support the clinical research of several faculty physicians. This is a unique opportunity to receive mentorship from faculty on the cutting edge of radiation oncology, work closely with research teams to produce world-class clinical research, and gain insight into academic medicine. The Assistant Clinical Research Coordinator will perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. General administrative support for the faculty, including managing calendars, scheduling meetings, and answering phone calls, is also required. The Assistant Clinical Research Coordinator will work under the direction and supervision of the faculty physician and radiation therapy division manager. Stanford University, located between San Francisco and San Jose in the heart of California's Silicon Valley, is one of the world's leading teaching and research universities. Since its opening in 1891, Stanford has been dedicated to finding solutions to big challenges and to preparing students for leadership in a complex world. Supporting that mission is a staff of more than 10,000, which is rooted in a culture of excellence and values innovation, collaboration, and life-long learning. To foster the talents and aspirations of our staff, Stanford offers career development programs, competitive pay that reflects market trends and benefits that increase financial stability and promote healthy, fulfilling lives. An award- winning employer, Stanford offers an exceptional setting for professionals looking to advance their careers. Duties include:
Research Duties (50%): Collect patient information by reviewing electronic medical records and organize data for analysis in retrospective research studies.Interface with patients in order to administer research questionnaires.Perform telephone or in-person interviews to gather data. Call patients for reminders or other requirements.Correspond with the Institution Review Board and the Cancer Clinical Trials Office in order to open, close, and renew research studies, register new patients consented for clinical trials, and submit adverse event and case report forms.Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.Assist in the preparation and publication of research abstracts and manuscripts by working with biostatisticians, residents, and faculty to analyze completed data and write up research findings.May be required to consent patients for blood draws in prospective research studies. May be required to prepare, process, and ship specimens and samples accurately under well-defined requirements.May work closely with and assist the Clinical Research Coordinators on prospective trials. Non-Research Duties (50%) Schedule meetings and interviews for faculty, update calendars, and reserve meeting locations.Arrange travel in compliance with department, university, and sponsor policies. Answer phone calls from patients and hospital support staff and forward to scheduling team and new patient coordinators. Communicate patients' concerns or questions to nurses and faculty.Submit expense reimbursements for faculty.Renew memberships and journal subscriptions for faculty.Assist in billing patients and insurers by filling out relevant documents.Retrieve and send faxes and routine correspondence regarding patient information and deliver scans to nurses.Send emails to team members, hospital staff, and faculty. Respond promptly to email correspondence. Duties may vary based on faculty's research studies. Applicants are required to upload a cover letter and resume to be considered for this opening.
* - Other duties may also be assigned DESIRED QUALIFICATIONS: Four year college degree in a related field.Prior clinical or research experience, including undergraduate experience.Experience with project management or coordination.Experience working with healthcare professionals and clinical research participants. Experience with University related research policies and procedures. EDUCATION & EXPERIENCE (REQUIRED):
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
- Two year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.
CERTIFICATIONS & LICENSES:
- General knowledge of medical terminology.
PHYSICAL REQUIREMENTS*: Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. * - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
- Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.
WORKING CONDITIONS: Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.May require extended or unusual work hours based on research requirements and business needs.
Location: School of Medicine
To be considered for this position please visit our web site and apply on line at the following link: stanfordcareers.stanford.edu
Stanford is an equal opportunity employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law.